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前列腺癌基因表达谱芯片的生物信息学分析 被引量:4

An integrative bioinformatics study of gene expression profile in prostate cancer
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摘要 目的利用生物信息学方法分析前列腺癌基因表达谱芯片,研究前列腺癌差异表达基因的功能及调控网络。方法采用GEO数据库中获取的前列腺癌基因表达谱芯片数据,利用R软件及affy、limma、pheatmap、ggplot2等R软件包进行数据挖掘及生物信息学分析。结合生物信息学工具DAVID、Gene MANIA对差异表达基因及其调控网络进行分析。结果共筛选出前列腺癌与癌旁组织差异表达基因56个,表达上调15个,表达下调41个,前列腺癌与癌旁组织的差异表达基因被富集到不同的子集。其中cav1、slc16a2、cav2、slc16a5、magi2、ptrf、pdlim5、lmod1、abcc6等9个基因被富集到"细胞功能"分类下的"细胞膜组分"子集中,其中cav1、cav2、ptrf影响细胞膜内陷囊状结构的功能,可能在前列腺癌发生发展中发挥重要作用。结论前列腺癌与癌旁组织的差异表达基因之间存在复杂的调控网络,生物信息学可以从中提取有效信息,为前列腺癌分子机制研究提供思路及数据基础。 Objective To analyze gene expression profile for exploring the function and regulatory network of differentially expressed genes in prostate cancer by bioinformatics. Methods The data of gene expression profile in prostate cancer were obtained from GEO database. R software and affy, limma, pheatmap, ggplot2 and other R packages were applied for data mining and bioinformatics analysis. Combined with DAVID and GeneMANIA , dif- ferentially expressed genes and their regulatory networks were annotated. Results These differentially expressed genes with statistical significance were 56 genes, 15 upregulated genes, 41 downregulated genes; these genes were enriched into different subgroups, cavl , slcl6a2, car2, slcl6a5 , magi2, ptrf , pdlim5 , lmodl and abcc6 were en- riched into the "cell membrane component" subgroup of "cell component" category, carl, cav2 and pttf regulated the function of caveolae, they may play an important role in the occurrence and development of prostate cancer. Conclusion Differentially expressed genes between prostate cancer and adjacent tissues assemble a complex regulatory network. Bioinformatics is a tool for data mining of the regulatory network , which provides ideas and data for the molecular mechanisms in prostate cancer.
出处 《安徽医科大学学报》 CAS 北大核心 2017年第2期199-202,共4页 Acta Universitatis Medicinalis Anhui
基金 国家重点基础研究发展计划(973计划)项目(编号:2014CB745200) 国家自然科学基金(编号:81301740)
关键词 前列腺癌 基因表达谱 生物信息学 prostate cancer gene expression profile bioinformatics
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  • 1Ryan C J, Smith M R, de Bono J S, et al. Abiraterone in meta- static prostate cancer without previous chemotherapy[J].N Engl J Med, 2013, 368(2):138-48.
  • 2Loblaw D A, Walker-Dilks C, Winquist E, et al. Systemic thera- py in men with metastatic castration-resistant prostate cancer: a systematic review[J]. Clin Oncol (R Coll Radiol), 2013, 25 (7) :406 -30.
  • 3Tai S, Sun Y, Squires J M, et al. PC3 is a cell line characteristic of prostatic small cell carcinoma[J]. Prostate, 2011 , 71 ( 15 ) : 1668 - 79.
  • 4Xu J, Mo Z, Ye D, et al. Genome-wide association study in Chi- nese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4[J]. NatGenet, 2012, 44(11) :1231 -5.
  • 5Scher H I, Fizazi K, Saad F, et al. Increased survival with enz- alutamide in prostate cancer after chemotherapy [ J ]. N Engl J Med, 2012, 367(13) :1187 -97.
  • 6Lian J, Wu X, He F, et al. A natural BH3 mimetic induces auto- phagy in apoptosis-resistant prostate cancer via modulating Bcl-2- Beclinl interaction at endoplasmic reticulum[ J]. Cell Death Dif- fer, 2011, 18(1) :60 -71.
  • 7de Bono J S, Logothetis C J, Molina A, et al. Abiralerone and in- creased survival in metastatic prostate cancer[ J]. N Engl J Med, 2011, 364 ( 21 ) : 1995 - 2005.
  • 8Kaini R R, Sillerud L O, Zhaorigetu S, et al. Autophagy regulates lipolysis and cell survival through lipid droplet degradation in an- drogen-sensitive prostate cancer cells [ J ]. Prostate, 2012, 72 (13) :1412 -22.
  • 9Turner L S, Cheng J C, Beckham T H, et al. Autophagy is in- creased in prostale cancer cells overexpressing acid ceramidase and enhances resistance to C6 ceramide[ J ]. Prostate Cancer Prostatic Dis, 2011 , 14(1) :30 -7.
  • 10Lozy F, Karantza V. Autophagy and cancer cell metabolism [ J]. Semin Cell Dev Biol,2011, 23(4) :395 -401.

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